Job Category: Regulatory Affairs Job Description: Job Summary : Regulatory Affairs Specialist is responsible... for obtaining and documenting our mission-critical, domestic regulatory clearances for Masimo's amazing innovative products. The...
), Regulatory Compliance Review, Regulatory Affairs · Perform global regulatory compliance review of essential documents... country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management Good...
Overview The Regulatory Affairs Specialist II has primary responsibility for provision of In Vitro Diagnostic...: Maintaining / Sustaining regulatory filings Act as regulatory affairs lead for filing regulatory submissions for existing...
you should apply if you have: CA / MBA Finance with 8+ years of experience in a senior compliance, regulatory affairs or advisory role in payments, banking... maintain up to date regulatory obligations framework and CRED's manner of compliances to those obligations act as consultant...
in the field, supply chain, regulatory affairs, marketing and all other interfering interfaces. Also, you continuously.... You are the entry point for the first level commercial and regulatory questions from our internal and external clients received...
metrics and drive performance improvements. Liaise with Regulatory affairs on status of registration and licenses. Work...
compliance with regulatory standards is crucial. Proficiency in key accounting concepts-such as accruals, amortization... Ministry of Home Affairs (MHA). Employee Development: Organize and deliver regular training sessions for employees, addressing...
, and traceability in Teva's publication tracking tool. Ability to adapt writing style for varied audiences such as specialist.... Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams (internally and externally...
, and traceability in Teva's publication tracking tool. Ability to adapt writing style for varied audiences such as specialist.... Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams (internally and externally...
, and traceability in Teva's publication tracking tool. Ability to adapt writing style for varied audiences such as specialist.... Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams (internally and externally...
. Collaborates closely with cross-functional teams including Eng. manufacturing, regulatory affairs. Responsible for defining... to new team members Ensure medical devices meet the highest standards of safety, efficacy, and regulatory compliance...